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猪气管中UDP-半乳糖:2-乙酰氨基-2-脱氧-D-葡萄糖3-β-半乳糖基转移酶的特性分析

Characterization of UDP-galactose:2-acetamido-2-deoxy-D-glucose 3 beta-galactosyltransferase from pig trachea.

作者信息

Sheares B T, Carlson D M

出版信息

J Biol Chem. 1983 Aug 25;258(16):9893-8.

PMID:6411707
Abstract

We have previously reported the enzymatic synthesis of galactosyl-beta 1,3-N-acetylglucosamine using membrane preparations from pig trachea (Sheares, B. T., Lau, J. T. Y., and Carlson, D. M. (1982) J. Biol. Chem. 257, 599-602). The enzyme catalyzing the synthesis of this disaccharide, UDP-galactose:N-acetylglucosamine 3 beta-galactosyltransferase, has been solubilized and contaminating galactosyltransferases, including the UDP-galactose:N-acetylglucosamine 4 beta-galactosyltransferase and the UDP-galactose:N-acetylgalactosamine-mucin 3 beta-galactosyltransferase, were removed by affinity chromatography on alpha-lactalbumin-agarose, N-acetylglucosamine-agarose, and asialo-ovine submaxillary mucin bound to DEAE-Sephacel. UDP-galactose:N-acetylglucosamine 3 beta-galactosyltransferase and a yet unidentified UDP-galactose:N-acetylglucosamine 4 beta-galactosyltransferase, both not retained by the alpha-lactalbumin-agarose, were further purified by adsorption to a UDP-hexanolamine-Sepharose column and these two galactosyltransferase activities were finally resolved by gel filtration on Sephacryl S-200. The purified UDP-galactose:N-acetylglucosamine 3 beta-galactosyltransferase displays an absolute requirement for a divalent cation (Mn2+ or Co2+) and is most active at pH 6.0. Unlike the UDP-galactose:N-acetylglucosamine 4 beta-galactosyltransferase, UDP-galactose:N-acetylglucosamine 3 beta-galactosyltransferase is not inhibited by high concentrations of N-acetylglucosamine. Apparent Km values are UDP-galactose, 0.23 mM, and N-acetylglucosamine, 385 mM. The apparent Km for a synthetic acceptor, N-acetylglucosaminyl-beta 1, 3-N-acetylgalactosamine-O-benzyl, was 2.4 mM. Acceptor specificity suggests that this 3 beta-galactosyltransferase is responsible for elongation of oligosaccharide chains in mucin glycoproteins and in glycolipids.

摘要

我们之前报道过利用猪气管的膜制剂酶促合成β-1,3-半乳糖基-N-乙酰葡糖胺(Sheares, B. T., Lau, J. T. Y., and Carlson, D. M. (1982) J. Biol. Chem. 257, 599 - 602)。催化这种二糖合成的酶,即UDP-半乳糖:N-乙酰葡糖胺3β-半乳糖基转移酶,已被溶解,并且包括UDP-半乳糖:N-乙酰葡糖胺4β-半乳糖基转移酶和UDP-半乳糖:N-乙酰半乳糖胺-粘蛋白3β-半乳糖基转移酶在内的污染性半乳糖基转移酶,通过在α-乳白蛋白-琼脂糖、N-乙酰葡糖胺-琼脂糖以及结合于DEAE-葡聚糖凝胶的去唾液酸羊颌下粘蛋白上进行亲和层析而被去除。UDP-半乳糖:N-乙酰葡糖胺3β-半乳糖基转移酶和一种尚未鉴定的UDP-半乳糖:N-乙酰葡糖胺4β-半乳糖基转移酶,两者都不被α-乳白蛋白-琼脂糖保留,通过吸附到UDP-己醇胺-琼脂糖柱上进一步纯化,并且这两种半乳糖基转移酶活性最终通过在Sephacryl S - 200上进行凝胶过滤得以分离。纯化后的UDP-半乳糖:N-乙酰葡糖胺3β-半乳糖基转移酶对二价阳离子(Mn2 +或Co2 +)有绝对需求,并且在pH 6.0时活性最高。与UDP-半乳糖:N-乙酰葡糖胺4β-半乳糖基转移酶不同,UDP-半乳糖:N-乙酰葡糖胺3β-半乳糖基转移酶不受高浓度N-乙酰葡糖胺的抑制。表观Km值分别为:UDP-半乳糖,0.23 mM;N-乙酰葡糖胺,385 mM。对于合成受体N-乙酰葡糖胺基-β1,3-N-乙酰半乳糖胺-O-苄基,表观Km为2.4 mM。受体特异性表明这种3β-半乳糖基转移酶负责粘蛋白糖蛋白和糖脂中寡糖链的延长。

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